Objectives: A previously unidentified mecA homologue, mecA LGA251 , has recently been described in methicillinresistant Staphylococcus aureus (MRSA) from humans and dairy cattle. The origin and epidemiology of this novel homologue are unclear. The objective of this study was to provide basic descriptive information of MRSA isolates harbouring mecA LGA251 from a range of host animal species.Methods: A number of S. aureus isolates from historical animal isolate collections were chosen for investigation based on their similarity to known mecA LGA251 MRSA isolates. The presence of mecA LGA251 was determined using a multiplex PCR and antimicrobial susceptibility testing performed by disc diffusion.Results: MRSA harbouring mecA LGA251 were found in isolates from a domestic dog, brown rats, a rabbit, a common seal, sheep and a chaffinch. All of the isolates were phenotypically MRSA, although this depended on which test was used; some isolates would be considered susceptible with certain assays. All isolates were susceptible to linezolid, rifampicin, kanamycin, norfloxacin, erythromycin, clindamycin, fusidic acid, tetracycline, trimethoprim/sulfamethoxazole and mupirocin. Five multilocus sequence types were represented (2273, 130, 425, 1764 and 1245) and six spa types (t208, t6293, t742, t6594, t7914 and t843). Conclusions:The discovery of MRSA isolates possessing mecA LGA251 from a diverse range of host species, including different taxonomic classes, has important implications for the diagnosis of MRSA in these species and our understanding of the epidemiology of this novel mecA homologue.

The incidence of the epidemic methicillin-resistant Staphylococcus aureus (EMRSA) strains EMRSA-15 and EMRSA-16 in Scotland has increased dramatically, now accounting for c. 70% and c. 20% of isolates, respectively. Epidemiological tracking of these EMRSA strains is difficult, as c. 50% of EMRSA-15 and c. 35% of EMRSA-16 isolates are indistinguishable using pulsed-field gel electrophoresis (PFGE) and other typing methods. The usefulness of mec-associated direct repeat unit (dru) sequence analysis as a more sensitive approach to tracking the persistence and spread of these 'clonal' EMRSA strains in Scotland was evaluated. Analysis of 47 EMRSA-15 and 57 EMRSA-16 isolates (including two separately cultured isolates of the Harmony collection type strain) obtained from 22 hospital laboratories over an 8-year period (1997-2005) revealed 13 and 12 different dru types, respectively. Whereas some types appeared to be endemic in multiple hospitals, subtypes that may represent specific strain movement among hospitals in a given geographical region were identified in other instances. These results suggest that mec-associated dru typing may have potential for identifying and tracking specific subtypes of otherwise indistinguishable epidemic MRSA isolates such as those in Scotland.

A study was conducted to ascertain the efficiency and effectiveness of an air filtration system (Electromedia Model 100C, Clean Air UK, UK) in the hospital ward. The sampling was conducted using a portable Surface Air Sampler (Cherwell Laboratories, Bicester, UK) in conjunction with settle plates. Samples were taken two days before and two days following activation of the filtration system and results compared. A clear, demonstrable, statistically significant reduction in microbial organisms following the activation of the filtration systems is evident (81% settle plates; 24% Surface Air Sampler). This study has implications for the improved health and welfare of patients and healthcare workers who may benefit through the implementation of such a system.

No abstract